Department of Health and Human Services' logo Department of Health and Human Services

Public Health Service
Food and Drug Administration
Florida District


555 Winderley Pl #200
Maitland, FL 32751

February 22, 2005

Ian Ramsay, President
Aiva Jade Enterprises, Inc.
6818 NW 20th Ave
Fort Lauderdale, FL 33309

Ref. No. FLA-05-19

Dear Mr Ramsay:

On November 4, 2004, FDA Investigator Sherbet Samuels inspected your firm at 6818 NW 20th Ave, Fort Lauderdale, FL. During the inspection, the investigator collected labeling for two products you manufacture and offer for sale, namely, Varisi The Formula for Clean and Healthy Nails, and Varisi Healthy Feet. We have also reviewed your Internet website at the following address: Our review reveals that your products are being marketed in violation of the Federal Food, Drug, and Cosmetic Act (the Act). You can find the Act and its implementing regulations on our Internet website at

Under Section 201(g)(1)(B) of the Act (21 USC 321(g)), articles intended for use in the diagnosis, cure, mitigation, treatment, of prevention of disease are drugs. The following claims on your products' labeling, including promotional materials entitled "Restore Problem Nails Healthy Feet" and "Restore Problem Nails" indicates that your products are intended to be used as drugs:

Intended use as a drug from website

Moreover, your promotional literature for Varisi The Formula for Clean and Healthy Nails also directs the reader to your website where this product's intended use is further established by referencing nail disorders, pictorial depictions of diseased nails, and the product's claimed ability to "exert a positive influence on nails that have been adversely affected by trauma…" Your website lists five types of traumas (i.e., chemical trauma, acute trauma, micro trauma, mechanical trauma, and non-traumatic diseases).


Furthermore, the following promotional claims for Varisi Healthy Feet appeared on your website at

New Drugs

Because the products are not generally recognized as safe and effective when used as labeled, they are also new drugs as defined in Section 201(p) of the Act (21 USC 321 (p). New drugs may not be legally marketed in the United States without prior approval from FDA as described in Section 505(a) of the Act (21 USC 355(a)).

OTC Monograph

The antifungal claims further document your product's intended use (i.e., to treat athlete's foot) as a drug as defined in Section 201(g)(1)(B) of the Act. Thus, in the absence of an approved new drug application under Section 505 of the Act, the product is subject to final regulations covering topical OTC antifungal drug products (21 CFR Part 333, Subpart C). Consequently, the product is misbranded under sections 502(e) and 502(f)(1) and (2) of the Act in that the product fails to bear a statement of identity, directions for use, and warnings as required by 21 CFR 333.250(a)-(d).

In addition, the product Varisi Healthy Feet is misbranded under section 502(c) of the Act in that the labeling of Varisi Healthy Feet fails to comply with the regulation covering the format and content of OTC drug labeling (21 CFR 201.66).

This letter is not an all-inclusive review of your promotional labeling, including your website and the products that your firm markets. It is your responsibility to ensure that all products marketed by your firm comply with the Act and its implementing regulations.

The Act authorizes the seizure of illegal products and injunctions against the manufacturers and distributors of those products. You should take prompt action to correct any violations identified in this letter. Failure to do so may result in enforcement action without further notice.

Please advise this office, in writing and within fifteen (15) working days of receipt of this letter, as to the specific steps that you have taken to correct any violations and to assure that similar violations do not occur. If corrective action cannot be completed with fifteen working days, state the reason for the delay and the time within which the corrections will be made.

Your reply should be addressed to Shari H. Shambaugh, Compliance Officer, US Food and Drug Administration, 555 Winderley Pl #200, Maitland, FL 32751.

Emma K. Singleton
District Director

This page was posted on March 28, 2006.

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